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Gene CSF3R
Variant P782Hfs*8
Impact List frameshift
Protein Effect unknown
Gene Variant Descriptions CSF3R P782Hfs*8 indicates a shift in the reading frame starting at amino acid 782 and terminating 8 residues downstream causing a premature truncation of the 836 amino acid Csf3r protein (UniProt.org). P782Hfs*8 has been identified in the scientific literature (PMID: 29932212), but has not been biochemically characterized and therefore, its effect on Csf3r protein function is unknown (PubMed, Feb 2024).
Associated Drug Resistance
Category Variants Paths

CSF3R mutant CSF3R P782Hfs*8

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Transcript NM_000760.4
gDNA chr1:g.36466523_36466524insTTGT
cDNA c.2344_2345insACAA
Protein p.P782Hfs*8
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000760.4 chr1:g.36466523_36466524insTTGT c.2344_2345insACAA p.P782Hfs*8 RefSeq GRCh38/hg38
NM_000760.3 chr1:g.36466523_36466524insTTGT c.2344_2345insACAA p.P782Hfs*8 RefSeq GRCh38/hg38

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References